Medtronic Sofamor Danek
Medtronic Sofamor Danek holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2021.
Top product codes for Medtronic Sofamor Danek
Recent clearances by Medtronic Sofamor Danek
1–100 of 154- K212428 — Centerpiece Plate Fixation System
- K201267 — Adaptix Interbody System with Titan nanoLOCK Surface Technology
- K173125 — T2 STRATOSPHERE Expandable Corpectomy System
- K172199 — ELEVATE Spinal System, CAPSTONE PTC Spinal System, CRESCENT Spinal System, CRESCENT Spinal System Titanium
- K171031 — CRESCENT Spinal System
- K171468 — FUSE Spinal System
- K170679 — CD HORIZON® Spinal System, Medtronic Reusable Instruments for Use with the IPC® POWEREASE® System, Medtronic Navigated Reusable Instruments for Use with the STEALTHSTATION® and IPC® POWEREASE® Systems
- K161210 — RIALTO(TM) SI Fusion System, Medtronic Reusable Instruments for Use with the IPC(TM) Powerease(TM) System, and Medtronic Navigated Manual Reusable Instruments for use with the StealthStation(TM) and IPC(TM) Powerease(TM) Systems
- K153373 — CORNERSTONE PSR Cervical Fusion System, PERIMETER C Spinal System, PEEK PREVAIL Cervical Interbody Device
- K140276 — CD HORIZON SPINAL SYSTEM
- K123246 — CD HORIZON SPIRE Z SPINAL SYSTEM
- K121982 — SOVEREIGN SPINAL SYSTEM
- K110472 — SI-FIX SACROILIAC JOINT FUSION SYSTEM
- K113529 — CD HORIZON VOYAGER SPINAL SYSTEM
- K113252 — PEEK PREVAIL CERVICAL INTERBODY DEVICE
- K111457 — CD HORIZON SPINAL SYSTEM
- K111525 — PERIMETER INTERBODY FUSION DEVICE
- K103731 — CAPSTONE R SPINAL SYSTEM
- K110676 — TSRH SPINAL SYSTEM
- K103049 — TSRH SPINAL SYSTEM
- K101772 — TSRH(R) SPINAL SYSTEM
- K091445 — CD HORIZON SPINAL SYSTEM
- K101168 — LEGEND POWER ADAPTER MODEL: 6475000
- K094042 — PEEK PREVAIL CERVICAL INTERBODY DEVICE
- K100214 — CORNERSTONE PSR CERVICAL INTERBODY FUSION DEVICE
- K100175 — CLYDESDALE SPINAL SYSTEM
- K091797 — TSRH SPINAL SYSTEM
- K094025 — CRESCENT SPINAL SYSTEM
- K093434 — VERTEX RECONSTRUCTION SYSTEM AND VERTEX SELECT RECONSTRUCTION SYSTEM
- K091813 — INTREPID SPINAL SYSTEM
- K090353 — PERIMETER INTERBODY FUSION DEVICE
- K090740 — MODIFICATION TO: TSRH SPINAL SYSTEM
- K091442 — CD HORIZON SPINAL SYSTEM
- K082166 — MASTERGRAFT STRIP
- K090390 — CD HORIZON SPINAL SYSTEM
- K090714 — VERTEX RECONSTRUCTION SYSTEM, VERTEX SELECT RECONSTRUCTION SYSTEM
- K082918 — MASTERGRAFT RESORBABLE CERAMIC GRANULES
- K082917 — MASTERGRAFT RESORBABLE CERAMIC GRANULES
- K083026 — CLYDESDALE SPINAL SYSTEM
- K082002 — PROGENIX PLUS
- K081080 — TSRH SPINAL SYSTEM
- K083071 — VERTEX RECONSTRUCTION SYSTEM
- K082463 — PROGENIX
- K082236 — CD HORIZON SPINAL SYSTEM
- K081784 — MASTERGRAFT PUTTY
- K082342 — MODIFICATION TO CAPSTONE SPINAL SYSTEM
- K082112 — T2 XVBR SPINAL SYSTEM
- K081038 — ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM
- K081297 — VERTEX RECONSTRUCTION SYSTEM
- K080462 — PROGENIX DBM PUTTY
- K080805 — MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
- K080083 — INTREPID SPINAL SYSTEM
- K072265 — PROGENIX DMB PUTTY
- K071942 — MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
- K071813 — MASTERGRAFT PUTTY
- K072429 — MODIFICATION TO TSRH SPINAL SYSTEM
- K070742 — MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
- K071033 — T2 XVBR SPINAL SYSTEM
- K063670 — MODIFICATIONS TO CD HORIZON SPINAL SYSTEM
- K070527 — ARCUATE VERTEBRAL AUGMENTATION SYSTEM
- K063248 — ARCUATE VERTEBRAL AUGMENTATION SYSTEM
- K063491 — T2 SCEPTOR SPINAL SYSTEM
- K063417 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K060415 — MODIFICATION TO: SATELLITE SPINAL SYSTEM
- K060794 — PROGENIX DBM PUTTY AND PASTE
- K060615 — CD HORIZON SPINAL SYSTEM
- K062606 — CD HORIZON SPINAL SYSTEM
- K062427 — VERTE-STACK SPINAL SYSTEM
- K061635 — MSD BIPOLAR FORCEPS
- K062073 — VERTE-STACK SPINAL SYSTEM
- K061579 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K061915 — CD HORIZON SPINAL SYSTEM
- K061304 — CD HORIZON SPINAL SYSTEM
- K061274 — VENTURE ANTERIOR CERVICAL PLATE SYSTEM
- K060719 — MODIFICATION TO VERTE-STACK SPINAL SYSTEM
- K060081 — BASIS SPINAL SYSTEM
- K060203 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K053474 — CD HORIZON SPINAL SYSTEM
- K053101 — CD HORIZON SPINAL SYSTEM
- K053483 — MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
- K052931 — MODIFICATION TO VERTE-STACK SPINAL SYSTEM
- K052747 — MODIFICATION TO:CD HORIZON SPINAL SYSTEM
- K052609 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K052734 — MODIFICATION TO: VERTEX RECONSTRUCTION SYSTEM
- K052376 — MODIFICATION TO: VERTEX RECONSTRUCTION SYSTEM
- K052402 — VERTEX RECONSTRUCTION SYSTEM
- K051320 — SATELLITE SPINAL SYSTEM
- K052144 — TSRH SPINAL SYSTEM
- K052180 — MODIFICATION TO VERTEX RECONSTRUCTION SYSTEM
- K052187 — MODIFICATION TO: CD HORIZON SPINAL SYSTEM
- K052054 — TSRH SPINAL SYSTEM
- K051105 — BASIS VERTEBRAL BODY SPACER
- K043053 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K043488 — MODIFICATION TO CD HORIZON SPINAL SYSTEM
- K043602 — QUADRANT RETRACTOR SYSTEM
- K050282 — MODIFICATION TO TSRH SPINAL SYSTEM
- K050117 — MODIFICATION TO PYRAMID ANTERIOR PLATE FIXATION SYSTEM
- K043321 — MODIFICATION TO: CD HORIZON SPINAL SYSTEM
- K031782 — GAPP GRAFT CONTIANMENT DEVICE ORTHOPEDICS
- K043151 — MODIFICATION TO: CD HORIZON SPINAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.